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240095001: Lipid storage myopathy (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
359705015 Lipid storage myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
629192012 Lipid storage myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Lipid storage myopathy Is a Metabolic myopathy true Inferred relationship Some
Lipid storage myopathy Is a Congenital anomaly of skeletal muscle false Inferred relationship Some
Lipid storage myopathy Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Lipid storage myopathy Is a Lipid storage disease true Inferred relationship Some
Lipid storage myopathy Finding site Skeletal muscle structure true Inferred relationship Some 2
Lipid storage myopathy Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Neutral lipid storage disease with myopathy (disorder) Is a True Lipid storage myopathy Inferred relationship Some
Genetic recurrent myoglobinuria (disorder) Is a True Lipid storage myopathy Inferred relationship Some
Autosomal dominant myoglobinuria (disorder) Is a True Lipid storage myopathy Inferred relationship Some

This concept is not in any reference sets

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